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Endotoxin, Epinephrine, and Ellagic Acid Effects on the Radiation-Sensitized Walker 256 Rat Carcinosarcoma
A radiation exposure of 1500 R to the Walker 256 rat tumor was found to sensitize this tumor to the effect of a sublethal dose of endotoxin (Sarratia marcescens lipopolysaccharide) given 2 days later so that complete or almost complete destruction of the tumor resulted. Histological study showed rap...
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Published in: | Radiation research 1968-10, Vol.36 (1), p.166-179 |
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creator | Ma. De Los Angeles Contreras Bale, William F. |
description | A radiation exposure of 1500 R to the Walker 256 rat tumor was found to sensitize this tumor to the effect of a sublethal dose of endotoxin (Sarratia marcescens lipopolysaccharide) given 2 days later so that complete or almost complete destruction of the tumor resulted. Histological study showed rapidly developing massive necrosis of tumor tissue. Tracer experiments with 131 I-labeled antibody to rat fibrin indicated an absence of blood circulation in the treated tumor. These results suggest that the lesion may be secondary to blood coagulation occurring in the vascular bed of the tumor. Apparently identical lesions were also produced by epinephrine and ellagic acid, alone or in combination. It is known that even untreated tumors are often the site of fibrin deposition. Presumably radiation, by injury to tumor cells, enhances the release of coagulation-producing substances into the vascular bed. It is postulated that the effect of subsequent treatment with the drugs listed above is produced by circulatory stasis induced in the tumor. This may be associated with Hageman factor activation or release of platelet factor 3. |
doi_str_mv | 10.2307/3572548 |
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De Los Angeles Contreras ; Bale, William F.</creator><creatorcontrib>Ma. De Los Angeles Contreras ; Bale, William F.</creatorcontrib><description>A radiation exposure of 1500 R to the Walker 256 rat tumor was found to sensitize this tumor to the effect of a sublethal dose of endotoxin (Sarratia marcescens lipopolysaccharide) given 2 days later so that complete or almost complete destruction of the tumor resulted. Histological study showed rapidly developing massive necrosis of tumor tissue. Tracer experiments with 131 I-labeled antibody to rat fibrin indicated an absence of blood circulation in the treated tumor. These results suggest that the lesion may be secondary to blood coagulation occurring in the vascular bed of the tumor. Apparently identical lesions were also produced by epinephrine and ellagic acid, alone or in combination. It is known that even untreated tumors are often the site of fibrin deposition. Presumably radiation, by injury to tumor cells, enhances the release of coagulation-producing substances into the vascular bed. It is postulated that the effect of subsequent treatment with the drugs listed above is produced by circulatory stasis induced in the tumor. This may be associated with Hageman factor activation or release of platelet factor 3.</description><identifier>ISSN: 0033-7587</identifier><identifier>EISSN: 1938-5404</identifier><identifier>DOI: 10.2307/3572548</identifier><identifier>PMID: 17387937</identifier><language>eng</language><publisher>United States: Academic Press, Inc</publisher><subject>Animals ; Antibodies ; Antineoplastics ; Blood ; Cancer ; Carcinoma - drug therapy ; Carcinoma - pathology ; Carcinoma - radiotherapy ; Combined Modality Therapy ; Dosage ; Dose-Response Relationship, Drug ; Ellagic Acid - administration & dosage ; Endotoxins ; Endotoxins - administration & dosage ; Epinephrine - administration & dosage ; Female ; Histology ; Necrosis ; Radiation Tolerance - drug effects ; Rats ; Rats, Sprague-Dawley ; Space life sciences ; Treatment Outcome ; Tumors</subject><ispartof>Radiation research, 1968-10, Vol.36 (1), p.166-179</ispartof><rights>Copyright 1968 Academic Press Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3572548$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3572548$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17387937$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ma. De Los Angeles Contreras</creatorcontrib><creatorcontrib>Bale, William F.</creatorcontrib><title>Endotoxin, Epinephrine, and Ellagic Acid Effects on the Radiation-Sensitized Walker 256 Rat Carcinosarcoma</title><title>Radiation research</title><addtitle>Radiat Res</addtitle><description>A radiation exposure of 1500 R to the Walker 256 rat tumor was found to sensitize this tumor to the effect of a sublethal dose of endotoxin (Sarratia marcescens lipopolysaccharide) given 2 days later so that complete or almost complete destruction of the tumor resulted. Histological study showed rapidly developing massive necrosis of tumor tissue. Tracer experiments with 131 I-labeled antibody to rat fibrin indicated an absence of blood circulation in the treated tumor. These results suggest that the lesion may be secondary to blood coagulation occurring in the vascular bed of the tumor. Apparently identical lesions were also produced by epinephrine and ellagic acid, alone or in combination. It is known that even untreated tumors are often the site of fibrin deposition. Presumably radiation, by injury to tumor cells, enhances the release of coagulation-producing substances into the vascular bed. It is postulated that the effect of subsequent treatment with the drugs listed above is produced by circulatory stasis induced in the tumor. This may be associated with Hageman factor activation or release of platelet factor 3.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Antineoplastics</subject><subject>Blood</subject><subject>Cancer</subject><subject>Carcinoma - drug therapy</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma - radiotherapy</subject><subject>Combined Modality Therapy</subject><subject>Dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>Ellagic Acid - administration & dosage</subject><subject>Endotoxins</subject><subject>Endotoxins - administration & dosage</subject><subject>Epinephrine - administration & dosage</subject><subject>Female</subject><subject>Histology</subject><subject>Necrosis</subject><subject>Radiation Tolerance - drug effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Space life sciences</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><issn>0033-7587</issn><issn>1938-5404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1968</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLxDAUhYMozvjAfyBZiG6mmjZNky6HoT5gQPCBy5KmiZOxTWqSAfXXm2EKrtzcw-V-HO45AJyl6DrDiN5gQjOSsz0wTUvMEpKjfB9MEcI4oYTRCTjyfo3inhblIZikFDNaYjoF68q0NtgvbWawGrSRw8rFOYPctLDqOv6uBZwLHRelpAgeWgPDSsIn3moetDXJszReB_0jW_jGuw_pYEaKeA9wwZ3Qxvootucn4EDxzsvTUY_B6231srhPlo93D4v5MhFZSUMiFMNtwxTJMYv_UqlaInAp2owKikrUsKIRpUJprjjnTKGCKpVypAhBEsdUx-By5zs4-7mRPtS99kLGLEbaja9pgfOCsi14tQOFs947qerB6Z677zpF9bbWeqw1kuej5abpZfvHjT1G4GIHrH2w7l-fX_MyfNY</recordid><startdate>196810</startdate><enddate>196810</enddate><creator>Ma. De Los Angeles Contreras</creator><creator>Bale, William F.</creator><general>Academic Press, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>196810</creationdate><title>Endotoxin, Epinephrine, and Ellagic Acid Effects on the Radiation-Sensitized Walker 256 Rat Carcinosarcoma</title><author>Ma. De Los Angeles Contreras ; Bale, William F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c297t-cf83db8f54380317efd5c39cd27c7090b86bc9f014faaa8f067ff1a0f550e3793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1968</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Antineoplastics</topic><topic>Blood</topic><topic>Cancer</topic><topic>Carcinoma - drug therapy</topic><topic>Carcinoma - pathology</topic><topic>Carcinoma - radiotherapy</topic><topic>Combined Modality Therapy</topic><topic>Dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>Ellagic Acid - administration & dosage</topic><topic>Endotoxins</topic><topic>Endotoxins - administration & dosage</topic><topic>Epinephrine - administration & dosage</topic><topic>Female</topic><topic>Histology</topic><topic>Necrosis</topic><topic>Radiation Tolerance - drug effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Space life sciences</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ma. De Los Angeles Contreras</creatorcontrib><creatorcontrib>Bale, William F.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Radiation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ma. De Los Angeles Contreras</au><au>Bale, William F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endotoxin, Epinephrine, and Ellagic Acid Effects on the Radiation-Sensitized Walker 256 Rat Carcinosarcoma</atitle><jtitle>Radiation research</jtitle><addtitle>Radiat Res</addtitle><date>1968-10</date><risdate>1968</risdate><volume>36</volume><issue>1</issue><spage>166</spage><epage>179</epage><pages>166-179</pages><issn>0033-7587</issn><eissn>1938-5404</eissn><abstract>A radiation exposure of 1500 R to the Walker 256 rat tumor was found to sensitize this tumor to the effect of a sublethal dose of endotoxin (Sarratia marcescens lipopolysaccharide) given 2 days later so that complete or almost complete destruction of the tumor resulted. Histological study showed rapidly developing massive necrosis of tumor tissue. Tracer experiments with 131 I-labeled antibody to rat fibrin indicated an absence of blood circulation in the treated tumor. These results suggest that the lesion may be secondary to blood coagulation occurring in the vascular bed of the tumor. Apparently identical lesions were also produced by epinephrine and ellagic acid, alone or in combination. It is known that even untreated tumors are often the site of fibrin deposition. Presumably radiation, by injury to tumor cells, enhances the release of coagulation-producing substances into the vascular bed. It is postulated that the effect of subsequent treatment with the drugs listed above is produced by circulatory stasis induced in the tumor. This may be associated with Hageman factor activation or release of platelet factor 3.</abstract><cop>United States</cop><pub>Academic Press, Inc</pub><pmid>17387937</pmid><doi>10.2307/3572548</doi><tpages>14</tpages></addata></record> |
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issn | 0033-7587 1938-5404 |
language | eng |
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source | JSTOR Archival Journals and Primary Sources Collection |
subjects | Animals Antibodies Antineoplastics Blood Cancer Carcinoma - drug therapy Carcinoma - pathology Carcinoma - radiotherapy Combined Modality Therapy Dosage Dose-Response Relationship, Drug Ellagic Acid - administration & dosage Endotoxins Endotoxins - administration & dosage Epinephrine - administration & dosage Female Histology Necrosis Radiation Tolerance - drug effects Rats Rats, Sprague-Dawley Space life sciences Treatment Outcome Tumors |
title | Endotoxin, Epinephrine, and Ellagic Acid Effects on the Radiation-Sensitized Walker 256 Rat Carcinosarcoma |
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